Variant report

Variant	rs1223042
Chromosome Location	chr6:102414229-102414230
allele	A/G
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

Extended variants
information (count: 53 )
Associated
traits (count: 0)

rSNPs within LD-proxies of this variant (count:47)

rs_ID	r²[population]
rs1223052	0.81[CEU][hapmap];0.94[YRI][hapmap]
rs1310715	0.96[CEU][hapmap];0.95[CHB][hapmap];1.00[JPT][hapmap];0.93[YRI][hapmap]
rs13190892	0.82[EUR][1000 genomes];0.87[ASN][1000 genomes]
rs13191478	0.95[CHB][hapmap];0.95[JPT][hapmap];0.82[EUR][1000 genomes];0.87[ASN][1000 genomes]
rs13191957	0.82[EUR][1000 genomes];0.87[ASN][1000 genomes]
rs13195038	0.95[CHB][hapmap];0.95[JPT][hapmap];0.82[EUR][1000 genomes];0.87[ASN][1000 genomes]
rs13197158	0.82[EUR][1000 genomes];0.87[ASN][1000 genomes]
rs13197283	0.82[EUR][1000 genomes];0.87[ASN][1000 genomes]
rs13198865	0.83[EUR][1000 genomes]
rs13199079	1.00[CHB][hapmap];0.95[JPT][hapmap];0.82[EUR][1000 genomes];0.87[ASN][1000 genomes]
rs13200524	0.95[CHB][hapmap];0.95[JPT][hapmap];0.82[EUR][1000 genomes];0.87[ASN][1000 genomes]
rs13201987	0.82[EUR][1000 genomes];0.87[ASN][1000 genomes]
rs13203019	0.82[EUR][1000 genomes];0.86[ASN][1000 genomes]
rs13203156	0.95[CHB][hapmap];0.95[JPT][hapmap];0.82[EUR][1000 genomes];0.87[ASN][1000 genomes]
rs13208276	0.84[CEU][hapmap];1.00[CHB][hapmap];0.95[JPT][hapmap]
rs13210850	0.82[EUR][1000 genomes];0.87[ASN][1000 genomes]
rs13210976	0.82[EUR][1000 genomes];0.87[ASN][1000 genomes]
rs13211215	0.82[EUR][1000 genomes];0.87[ASN][1000 genomes]
rs13215171	0.83[ASN][1000 genomes]
rs13216974	0.82[EUR][1000 genomes];0.87[ASN][1000 genomes]
rs13218403	0.80[CEU][hapmap];0.95[CHB][hapmap];0.95[JPT][hapmap];0.81[EUR][1000 genomes];0.87[ASN][1000 genomes]
rs1335022	0.95[CHB][hapmap];0.95[JPT][hapmap];0.82[EUR][1000 genomes];0.87[ASN][1000 genomes]
rs1335024	1.00[CHB][hapmap];0.95[JPT][hapmap];0.82[EUR][1000 genomes];0.87[ASN][1000 genomes]
rs1335031	0.83[CHB][hapmap]
rs1335033	0.82[CHB][hapmap]
rs2023599	0.83[CHB][hapmap]
rs2399584	0.88[CEU][hapmap];1.00[CHB][hapmap];0.95[JPT][hapmap]
rs2518146	0.80[CHB][hapmap]
rs2518148	0.82[CHB][hapmap]
rs2782908	0.96[CEU][hapmap];1.00[CHB][hapmap];1.00[JPT][hapmap]
rs2782929	0.85[CHB][hapmap]
rs2852607	0.80[CEU][hapmap];0.95[CHB][hapmap];0.91[JPT][hapmap]
rs2852608	0.82[CHB][hapmap]
rs35306110	0.81[EUR][1000 genomes];0.87[ASN][1000 genomes]
rs35697470	0.81[EUR][1000 genomes];0.87[ASN][1000 genomes]
rs62423079	0.83[EUR][1000 genomes];0.87[ASN][1000 genomes]
rs62423081	0.82[EUR][1000 genomes];0.87[ASN][1000 genomes]
rs62423082	0.82[EUR][1000 genomes];0.87[ASN][1000 genomes]
rs66829771	0.82[EUR][1000 genomes];0.88[ASN][1000 genomes]
rs67501069	0.81[EUR][1000 genomes];0.87[ASN][1000 genomes]
rs7738614	0.91[CHB][hapmap];0.95[JPT][hapmap];0.85[ASN][1000 genomes]
rs7749722	0.95[CHB][hapmap];0.95[JPT][hapmap];0.82[EUR][1000 genomes];0.86[ASN][1000 genomes]
rs7756449	0.95[CHB][hapmap];0.95[JPT][hapmap]
rs9485585	0.91[CHB][hapmap];0.95[JPT][hapmap];0.84[ASN][1000 genomes]
rs9498801	0.87[CHB][hapmap];0.95[JPT][hapmap];0.85[ASN][1000 genomes]
rs966953	1.00[CHB][hapmap];1.00[JPT][hapmap]
rs995640	0.82[CHB][hapmap];0.81[JPT][hapmap]

Variant overlapped rSNPs/rCNVs (count:6 , 50 per page) page: 1

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	nsv1032499	chr6:102069885-102720998	Weak transcription Enhancers Flanking Active TSS Active TSS ZNF genes & repeats Bivalent Enhancer Strong transcription	TF binding region CpG island Chromatin interactive region lncRNA	2 gene(s)	inside rSNPs	diseases
2	nsv830743	chr6:102284082-102459192	Weak transcription Active TSS Enhancers Flanking Active TSS ZNF genes & repeats	TF binding region CpG island Chromatin interactive region	1 gene(s)	inside rSNPs	diseases
3	nsv886465	chr6:102318339-102466397	Enhancers Weak transcription Active TSS Flanking Active TSS ZNF genes & repeats	TF binding region CpG island Chromatin interactive region	1 gene(s)	inside rSNPs	diseases
4	nsv886466	chr6:102327303-102432398	Weak transcription Enhancers Active TSS Flanking Active TSS ZNF genes & repeats	TF binding region Chromatin interactive region	1 gene(s)	inside rSNPs	diseases
5	nsv470850	chr6:102343078-102595587	Enhancers Weak transcription Active TSS Flanking Active TSS ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA	2 gene(s)	inside rSNPs	diseases
6	nsv830744	chr6:102369761-102566737	Weak transcription Enhancers Active TSS Flanking Active TSS ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA	2 gene(s)	inside rSNPs	diseases

No data

Chromatin state (count:0 , 50 per page) page:

No data

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dbSNP/dbVar ID: rs12345 /nsv7879
a single nucleotide as 0-based coordinates: chr1:12345
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